SEARCH · Search USGS

Results for “Chemistry and Water”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

SourceResearch connectionFrom yearThrough year

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 433 records · Page 24Linked to original sources

USGS1998

Geohydrology of the Winchester Subbasin, Riverside County, California

The 20-square-mile Winchester structural subbasin is an alluvium-filled paleocanyon that is as much as 900 feet deep. The alluvial aquifer is composed of detrital material that generally ranges in size from clay to fine gravel; the fine and coarse materials are mixed in some places and inter- bedded in others. The apparent lenticularity of fine- and coarse-grained materials and differing water quality with depth indicate that the aquifer is partly or locally confined. A ground-water divide exists east of the town of Winchester. West of the divide, ground water moves toward and into the South Perris and the Menifee subbasins. East of the divide, ground water moves toward and into the Hemet subbasin. The components of flow direction in the Winchester?Hemet subbasins border area are complex: along the border, some water moves from the southwest corner of the Hemet subbasin into the Winchester subbasin and then eastward subparallel to the border before moving back into the Hemet subbasin. The direction of ground-water movement between the Winchester and Hemet subbasins, and the position of the ground-water divide in the central part of the Winchester subbasin, have changed with time. Prior to about 1974, ground water moved both eastward from the divide and westward from the Hemet subbasin toward a local depression of the water table caused by pumping in the eastern part of the Winchester subbasin. Comparison of spring 1970 and spring 1993 ground-water levels indicates a net rise of as much as 150 feet in the east end of the Winchester subbasin. For this same period, water levels rose about 3 to 20 feet in the western and central parts of the subbasin. Ground-water chemistry in the Winchester subbasin and adjacent subbasins varies areally and vertically. In general, sodium, calcium, chloride, and sulfate are dominant ions. Water quality is generally poor: dissolved-solids concentration exceeded 2,000 milligrams per liter throughout much of the subbasin and was highest west of the town of Winchester. Eastward along the subbasin axis (toward the Hemet subbasin), the dissolved-solids concentration decreases and the pH increases (generally greater than 7.0). Samples from two multiple-well monitoring sites at the west and east ends of the subbasin indicate that the best quality water (dissolved-solids concentrations of 395 and 483 milligrams per liter) is from the deepest wells (perforated near the alluvium- bedrock contact). Samples from the deeper wells in the eastern part of the Winchester subbasin are similar in water type to a sample from a well in the western part of the Hemet subbasin, which suggests that the water may have flowed from the Hemet subbasin; alternatively, the chemistry may reflect the influence of good-quality water flowing from the fractured bedrock basement to the alluvium in the eastern part of the Winchester subbasin. In addition, the potential problem of poor-quality water moving from the Winchester subbasin into the Hemet subbasin may not exist at all depths; fair- to good-quality water may be present below a depth of about 450 feet. Dissolved-solids concentrations in the southwest part of the Hemet subbasin ranged from about 900 milligrams per liter at well 5S/1W-19Q1 about one-quarter mile north of the Winchester?Hemet subbasin boundary to about 3,500 milligrams per liter at well 5S/2W-24C2 near the bedrock outcrops southeast of the Lakeview Mountains. High dissolved-solids concentration in the vicinity of well 5S/2W-24C2 most likely is a result of dissolution of constituents from the aquifer matrix, evaporative processes, and agricultural practices that occur in that vicinity rather than a result of flow from the Winchester subbasin. Aquifer-test results indicate that the transmissivity is about 950 feet squared per day in the eastern part of the Winchester subbasin near the boundary with the Hemet subbasin and about 72 feet squared per day in the western part of the subbasin near the boundary with th

California↗

USGS1996

Theoretical considerations and a simple method for measuring alkalinity and acidity in low-pH waters by gran titration

Titrations for alkalinity and acidity using the technique described by Gran (1952, Determination of the equivalence point in potentiometric titrations, Part II: The Analyst, v. 77, p. 661-671) have been employed in the analysis of low-pH natural waters. This report includes a synopsis of the theory and calculations associated with Gran's technique and presents a simple and inexpensive method for performing alkalinity and acidity determinations. However, potential sources of error introduced by the chemical character of some waters may limit the utility of Gran's technique. Therefore, the cost- and time-efficient method for performing alkalinity and acidity determinations described in this report is useful for exploring the suitability of Gran's technique in studies of water chemistry.

Water-Resources Investigations Report↗

USGS2012

Hydrochemical evolution of sodium-sulfate and sodium-chloride groundwater beneath the Northern Chihuahuan Desert, Trans-Pecos, Texas, USA

Groundwater beneath the northern Chihuahuan Desert, Trans-Pecos, Texas, USA, occurs in both carbonate and siliciclastic aquifers beneath a thick unsaturated zone in shallow Rio Grande alluvium. Groundwater hydrochemical evolution was investigated by analyzing soils, soils leachates, bolson-fill sediments, water from the unsaturated zone, and groundwater from three major aquifers. Ionic relations, mineral saturation states, and geochemical modeling show that groundwater compositions are controlled by reactions in the unsaturated zone, mineralogy of unsaturated sediments and aquifers, position in the groundwater flow system, and extensive irrigation. Recharge to aquifers unaffected by irrigation is initially a Ca-HCO 3 type as a result of dissolving carbonate surficial salts. With continued flow and mineral-water interaction, saturation with calcite and dolomite is maintained, gypsum is dissolved, and aqueous Ca and Mg are exchanged for adsorbed Na to produce a Na-SO 4 water. Groundwater in Rio Grande alluvium is a Na-Cl type, reflecting river-water composition and the effects of irrigation, evapotranspiration, and surficial salt recycling. These results document two hydrochemical evolution paths for groundwater in arid lands. If recharge is dilute precipitation, significant changes in water chemistry can occur in unsaturated media, ion exchange can be as important as dissolution-precipitation reactions in determining groundwater composition, and mineral-water reactions ultimately control groundwater composition. If recharge is return flow of irrigation water that already contains appreciable solutes, mineral-water reactions are less important than irrigation-water composition in determining groundwater chemistry.

Hydrogeology Journal↗

USGS2019

Using stream-side groundwater discharge for geochemical exploration in mountainous terrain

Groundwater chemistry has been predominantly used in geochemical exploration studies to identify mineralized targets concealed under transported cover in areas with gentle topography. Another potentially valuable ap-plication that has received little attention is using groundwater chemistry to identify deposits concealed within mountain ridges. A number of geochemical exploration studies have employed surface water chemistry in hilly and mountainous terrain and have demonstrated mixed success. However, groundwater chemistry is potentially a more reﬁned and powerful tool because groundwater sample locations can be selected to target a speciﬁc hillslope zone, whereas surface water integrates the geochemical signature of the entire watershed area above the sample site. In this study, we propose an approach that utilizes shallow groundwater samples collected from near-stream, hand-installed sampling points. We tested this approach in Handcart Gulch, an unmined catchment in the Montezuma Mining District, Colorado, USA, where previous studies suggested the possible presence of a concealed mineral occurrence. Seventeen near-stream mini-boreholes were drilled in a stream-parallel 3.3-km-long transect to depths of ~2 m in ferricrete (iron-oxide cemented colluvium and alluvium) using a handheld rock-coring drill. Groundwater in the mini-boreholes was sampled for major and trace element chemistry, as well as environmental tracers including stable water isotopes, dissolved noble gases, helium isotopes, and tritium, to identify possible variations in groundwater age and recharge conditions/sources. Chemistry data delineate a well-deﬁned 900-m-wide zone of elevated SO4, Cu, and other metal concentrations on the east side of the stream. In this zone, Cu concentrations up to 2670 μg/L are 1–3 orders of magnitude greater than concentrations in upstream and downstream areas. Environmental tracer data show no corresponding anomalies in groundwater age or recharge conditions/sources within the zone, suggesting that the source of the elevated metals is a change in bedrock mineralogy as opposed to other hydrologic factors. The groundwater samples therefore successfully identify and reﬁne the location of a potential concealed high-Cu mineral occurrence in the watershed, de-monstrating that near-stream groundwater discharge may be a valuable medium for geochemical exploration in mountainous areas.

Colorado↗

USGS2015

Impact of wastewater infrastructure upgrades on the urban water cycle: Reduction in halogenated reaction byproducts following conversion from chlorine gas to ultraviolet light disinfection

The municipal wastewater treatment facility (WWTF) infrastructure of the United States is being upgraded to expand capacity and improve treatment, which provides opportunities to assess the impact of full-scale operational changes on water quality. Many WWTFs disinfect their effluent prior to discharge using chlorine gas, which reacts with natural and synthetic organic matter to form halogenated disinfection byproducts (HDBPs). Because HDBPs are ubiquitous in chlorine-disinfected drinking water and have adverse human health implications, their concentrations are regulated in potable water supplies. Less is known about the formation and occurrence of HDBPs in disinfected WWTF effluents that are discharged to surface waters and become part of the de facto wastewater reuse cycle. This study investigated HDBPs in the urban water cycle from the stream source of the chlorinated municipal tap water that comprises the WWTF inflow, to the final WWTF effluent disinfection process before discharge back to the stream. The impact of conversion from chlorine-gas to low-pressure ultraviolet light (UV) disinfection at a full-scale (68,000 m 3 d −1 design flow) WWTF on HDBP concentrations in the final effluent was assessed, as was transport and attenuation in the receiving stream. Nutrients and trace elements (boron, copper, and uranium) were used to characterize the different urban source waters, and indicated that the pre-upgrade and post-upgrade water chemistry was similar and insensitive to the disinfection process. Chlorinated tap water during the pre-upgrade and post-upgrade samplings contained 11 (mean total concentration = 2.7 μg L −1 ; n=5) and 10 HDBPs (mean total concentration = 4.5 μg L −1 ), respectively. Under chlorine-gas disinfection conditions 13 HDBPs (mean total concentration = 1.4 μg L −1 ) were detected in the WWTF effluent, whereas under UV disinfection conditions, only one HDBP was detected. The chlorinated WWTF effluent had greater relative proportions of nitrogenous, brominated, and iodinated HDBPs than the chlorinated tap water. Conversion of the WWTF to UV disinfection reduced the loading of HDBPs to the receiving stream by >90%.

Science of the Total Environment↗

USGS1997

Fe-Ca-phosphate, Fe-silicate, and Mn-oxide minerals in concretions from the Monterey Formation

Concentrically zoned phosphatic-enriched concretions were collected at three sites from the Monterey Formation. The following minerals were identified: vivianite, lipscombite, rockbridgeite, leucophosphite, mitridatite, carbonate fluorapatite, nontronite, todorokite, and barite. The mineralogy of the concretions was slightly different at each of the three collection sites. None of the concretions contains all of the minerals, but the spatial distribution of minerals in individual concretions, overlapping mineralogies between different concretions, and the geochemical properties of the separate minerals suggest a paragenesis represented by the above order. Eh increased from the precipitation of vivianite to that of rockbridgeite/lipscombite. The precipitation of leucophosphite, then mitridatite, carbonate fluorapatite and todorokite/Fe-oxide indicates increasing pH. Concretion growth culminated with the precipitation of todorokite, a Mn oxide, and minor amounts of barite along microfractures. Conspicuously absent are Fe-sulfide and Mn-phosphate minerals. The concretions are hosted by finely laminated diatomite. The laminations exhibit little to no deformation around the concretions, requiring that the concretions formed after compaction. We interpret this sediment feature and the paragenesis as recording the evolving pore-water chemistry as the formation was uplifted into the fresh-ground-water zone.

Chemical Geology↗

USGS2000

Calcite crystal growth inhibition by humic substances with emphasis on hydrophobic acids from the Florida Everglades

The crystallization of calcium carbonate minerals plays an integral role in the water chemistry of terrestrial ecosystems. Humic substances, which are ubiquitous in natural waters, have been shown to reduce or inhibit calcite crystal growth in experiments. The purpose of this study is to quantify and understand the kinetic effects of hydrophobic organic acids isolated from the Florida Everglades and a fulvic acid from Lake Fryxell, Antarctica, on the crystal growth of calcite (CaCO 3 ). Highly reproducible calcite growth experiments were performed in a sealed reactor at constant pH, temperature, supersaturation (Ω = 4.5), P CO 2 (10 −3.5 atm), and ionic strength (0.1 M) with various concentrations of organic acids. Higher plant-derived aquatic hydrophobic acids from the Everglades were more effective growth inhibitors than microbially derived fulvic acid from Lake Fryxell. Organic acid aromaticity correlated strongly with growth inhibition. Molecular weight and heteroatom content correlated well with growth inhibition, whereas carboxyl content and aliphatic nature did not.

Florida↗

USGS2019

Assessing the lead solubility potential of untreated groundwater of the United States

In the U.S., about 44 million people rely on self-supplied groundwater for drinking water. Because most self-supplied homeowners do not treat their water to control corrosion, drinking water can be susceptible to lead (Pb) contamination from metal plumbing. To assess the types and locations of susceptible groundwater, a geochemical reaction model that included pure Pb minerals and solid solutions of calcite (Ca x Pb 1– x CO 3 ) and apatite [Ca x Pb 5-x (PO 4 ) 3 (OH; Cl; F)] was developed to estimate the lead solubility potential (LSP) for over 8300 untreated groundwater samples collected from domestic and public-supply sites between 2000 and 2016 in the U.S. The LSP is the calculated amount of Pb metal that could dissolve at 25 °C before a Pb-bearing mineral precipitates. About 33% of untreated groundwater samples had LSP greater than 15 μg/L—the USEPA action level for dissolved plus particulate forms of Pb. Five percent of samples had high LSP (above 300 μg/L) and tended to occur in the eastern and southeastern U.S. Measured Pb concentrations above 15 μg/L were rarely detected (<1%) but always coincided with high LSP values. Future work will provide a better understanding of the relation between water chemistry, Pb-mineral formation, and dissolved Pb concentrations in tap water.

Environmental Science & Technology↗

USGS2008

Ground-water quality data in the coastal Los Angeles Basin study unit, 2006: Results from the California GAMA Program

Ground-water quality in the approximately 860 square-mile Coastal Los Angeles Basin study unit (CLAB) was investigated from June to November of 2006 as part of the Statewide Basin Assessment Project of the Ground-Water Ambient Monitoring and Assessment (GAMA) Program. The GAMA Statewide Basin Assessment was developed in response to the Ground-Water Quality Monitoring Act of 2001, and is being conducted by the U.S. Geological Survey (USGS) in cooperation with the California State Water Resources Control Board (SWRCB). The Coastal Los Angeles Basin study was designed to provide a spatially unbiased assessment of raw ground-water quality within CLAB, as well as a statistically consistent basis for comparing water quality throughout California. Samples were collected from 69 wells in Los Angeles and Orange Counties. Fifty-five of the wells were selected using a spatially distributed, randomized grid-based method to provide statistical representation of the study area (?grid wells?). Fourteen additional wells were selected to evaluate changes in ground-water chemistry or to gain a greater understanding of the ground-water quality within a specific portion of the Coastal Los Angeles Basin study unit ('understanding wells'). Ground-water samples were analyzed for: a large number of synthetic organic constituents [volatile organic compounds (VOCs), gasoline oxygenates and their degradates, pesticides, polar pesticides, and pesticide degradates, pharmaceutical compounds, and potential wastewater-indicators]; constituents of special interest [perchlorate, N-nitrosodimethylamine (NDMA), 1,4-dioxane, and 1,2,3-trichloropropane (1,2,3-TCP)]; inorganic constituents that can occur naturally [nutrients, major and minor ions, and trace elements]; radioactive constituents [gross-alpha and gross-beta radiation, radium isotopes, and radon-222]; and microbial indicators. Naturally occurring isotopes [stable isotopic ratios of hydrogen and oxygen, and activities of tritium and carbon-14] and dissolved noble gases also were measured to help identify the sources and ages of the sampled ground water. Quality-control samples (blanks, replicates, and samples for matrix spikes) were collected at approximately one-fourth of the wells, and the results for these samples were used to evaluate the quality of the data for the ground-water samples. Field blanks rarely contained detectable concentrations of any constituent, suggesting that contamination was not a significant source of bias. Differences between replicate samples were within acceptable ranges, indicating acceptably low variability. Matrix spike recoveries were within acceptable ranges for most compounds. Assessment of the quality-control information resulted in applying ?V? codes to approximately 0.1 percent of the data collected for ground-water samples (meaning a constituent was detected in blanks as well as the corresponding environmental data). This study did not attempt to evaluate the quality of drinking water delivered to consumers; after withdrawal from the ground, water typically is treated, disinfected, and (or) blended with other waters to maintain acceptable drinking-water quality. Regulatory thresholds are applied to the treated drinking water that is served to the consumer, not to raw ground water. However, to provide some context for the results, concentrations of constituents measured in the raw ground water were compared with regulatory and non-regulatory health-based thresholds established by the U.S. Environmental Protection Agency (USEPA), California Department of Public Health (CDPH, formerly California Department of Health Services [CADHS]) and thresholds established for aesthetic concerns (secondary maximum contaminant levels, SMCL-CA) by CDPH. Comparisons between data collected for this study and drinking-water thresholds are for illustrative purposes only, and are not indicative of compliance or non-compliance with those thresholds. VOCs were detected in alm

California↗

USGS2003

Surface-Water Quality of the Skokomish, Nooksack, and Green-Duwamish Rivers and Thornton Creek, Puget Sound Basin, Washington, 1995-98

Streamflow and surface-water-quality data were collected from November 1995 through April 1998 (water years 1996-98) from a surface-water network in the Puget Sound Basin study unit of the U.S. Geological Survey National Water-Quality Assessment program. Water samples collected monthly and during storm runoff events were analyzed for nutrients, major ions, organic carbon, and suspended sediment, and at selected sites, samples were analyzed for pesticides and volatile organic compounds. Eleven sites were established in three major watersheds--two in the Skokomish River Basin, three in the Nooksack River Basin, five in the Green-Duwamish River Basin, and one site in Thornton Creek Basin, a small tributary to Lake Washington. The Skokomish River near Potlatch, Nooksack River at Brennan, and Duwamish River at Tukwila are integrators of mixed land uses with the sampling sites locally influenced by forestry practices, agriculture, and urbanization, respectively. The remaining eight sites are indicators of relatively homogeneous land use/land cover in their basins. The site on the North Fork Skokomish River is an indicator site chosen to measure reference or background conditions in the study unit. In the Nooksack River Basin, the site on Fishtrap Creek is an indicator of agriculture, and the Nooksack River at North Cedarville is an indicator site of forestry practices in the upper watershed. In the Green-Duwamish River Basin, Springbrook Creek is an urban indicator, Big Soos Creek is an indicator of a rapidly developing suburban basin; Newaukum Creek is an indicator of agriculture; and the Green River above Twin Camp Creek is an indicator of forestry practices. Thornton Creek is an indicator of high-density urban residential and commercial development. Conditions during the first 18 months of sampling were dominated by above-normal precipitation. For the Seattle-Tacoma area, water year 1997 was the wettest of the 3 years during the sample-collection period. Nearly 52 inches fell (about 14 inches above average) and monthly precipitation was often 200 percent of normal. The wet years kept streamflows generally above normal and contributed to high concentrations of pesticides, nutrients, suspended sediment, and organic carbon in samples. On the basis of chemical concentrations, dissolved oxygen concentrations, and water temperature, the relative quality of water among the 11 study sites ranged from exceptionally high in the North Fork Skokomish and the Green to fair in Springbrook and Thornton. Water in the large rivers (Skokomish, Nooksack, Green-Duwamish) and in two of the small streams in the Puget Sound Lowlands (Big Soos and Newaukum) was characterized by dilute water chemistry with dissolved solids concentrations less than 130 milligrams per liter. Water in three other small streams in the Lowlands (Fishtrap, Springbrook, and Thornton) had dissolved solids concentrations as high as 320 milligrams per liter. Nutrient and pesticide concentrations mostly were higher in the small streams than in the large rivers. Suspended-sediment concentrations, however, were highest in the large rivers, with averages ranging from 85 to 443 milligrams per liter. During storm and flood events, suspended-sediment concentrations in samples from the Nooksack were as much as 2,800 milligrams per liter, and from the Skokomish, 1,500 milligrams per liter. Out of 86 pesticides and 86 volatile organic compounds analyzed, a total of 35 pesticides and 11 volatile organic compounds were detected at concentrations above laboratory reporting levels in samples collected from the four intensively studied sites, the lower Nooksack River, Duwamish River, Fishtrap Creek, and Thornton Creek. Herbicides were detected more frequently than insecticides. The herbicide prometon was detected in 66 percent of all 124 samples collected, followed by simazine (65 percent), atrazine (64 percent), and the insecticide diazinon (50 percent). The detected volatile organic c

Water-Resources Investigations Report↗

USGS1995

Chemical composition of ground water, hydrologic properties of basin-fill material, and ground-water movement in Salt Lake Valley, Utah

The chemical composition and movement of ground water and hydrologic properties of the basin‑fill material were studied to better under‑ stand the flow system in Salt Lake Valley, Utah. Recharge sources and water‑rock interactions influence the water chemistry in the principal and shallow unconfined aquifers. Chloride concentration in water from some wells has increased from the 1950’s and 1960’s to 1992, possibly because of the infiltration of water that contains dissolved road salt and the movement of ground water with relatively high chloride concentrations from volcanic rocks in the vicinity of these wells. Hydraulic‑conductivity values determined from slug tests done on wells finished in the shallow unconfined aquifer and confining layers ranged from 0.003 to 33.4 feet per day. Transmissivity values determined for the principal aquifer from four multiple‑well aquifer tests ranged from 6,400 to 43,600 feet squared per day. Vertical hydraulic‑conductivity values estimated from these tests are from 0.01 to 1 foot per day. Water from 81 sites was analyzed for the stable‑isotope ratios of oxygen and hydrogen to determine sources of recharge and mixing of water from these sources. Water sampled from the principal aquifer in the southeastern part of the valley is isotopically similar to water in Big and Little Cottonwood Creeks. Ground water sampled from the shallow unconfined aquifer is generally enriched in oxygen‑18 and deuterium relative to other water in the valley, except for water from the Jordan River and its diversions, which are probable recharge sources. Tritium concentrations ranging from about 33 to 59 tritium units in water from the principal aquifer in the southeastern part of the valley are representative of concentrations in water that was recharged in the 1960’s.

Utah↗

USGS1985

Geochemistry of ground-water in two sandstone aquifer systems in the Northern Great Plains in parts of Montana and Wyoming, North Dakota, and South Dakota

The Kootenai Formation in the Judith Basin, Montana, and the Lance Formation and Fox Hills Sandstone in the Powder River Basin, Wyoming, constitute two important sandstone aquifer systems in the Northern Great Plains region. Ground waters in each of these systems evolve from low dissolved-solids concentration, near-neutral pH, predominantly calcium and magnesium bicarbonate types in their recharge areas, to high dissolved-solids concentration, high pH, predominantly sodium-bicarbonate types in the basins. Oxidation potentials decrease as the waters flow downgradient under confined conditions. Calculation of the saturation states of aquifer minerals suggests several groups of mineral phases that could control ground- water chemistry. Mass transfer modeling indicates, however, that the observed behavior of major and minor dissolved species in both systems can satisfactorily be explained only by equilibration with cal cite, dolomite, or calcite and dolomite. The geochemistry of these systems is probably controlled by the incongruent dissolution of dolo mite to form calcite. This reaction appears to be driven by cation ex change and the dissolution of carbon dioxide. Plausible carbon diox ide sources include organic carbon oxidation and lignite coalification. Aluminosilicates influence major element chemistry primarily as sub trates for cation exchange, which, in combination with carbonate equilibria, buffer ground water pH at values of 8.5 to 8.9. Dissolved- iron concentrations are controlled by equilibration with amorphous ferric oxyhydroxides in oxidizing waters, with amorphous ferric oxyhydroxides and siderite in moderately reducing waters, and with siderite and amorphous ferrous sulfide in strongly reducing waters. Measured variations in dissolved carbonate isotopic composition compare favorably with carbon isotopic evolution, calculated by assuming dedolomitization. Recharge areas of the two systems are characterized by ground waters with high tritium and carbon-14 activities and relatively low dissolved-solids concentrations, with calcium and magnesium as the predominant cations. Recharge temperatures, calculated from dissolved-argon concentrations and 5 18 0 and SD isotopic measure ments, indicate that recharge is derived primarily from spring snow- melt rather than late spring and summer storms. Ground-water flow directions are generally parallel to trends of increasing dissolved solids concentrations and decreasing divalent to monovalent cation concentration ratios. However, these trends are sometimes obscured in areas of leakage or mixing. Further indication of leakage between aquifers is provided by abrupt changes in major element and isotopic chemistry, which are not characteristic of normally observed geo chemical evolution. Ground-water flow rates, calculated by adjusting measured carbon-14 activities for carbonate mass transfer, are com parable to values calculated from aquifer tests and potentiometric data. These carbon-14 flow rates average 1.6 meters per year for the Second Cat Creek sandstone of the Kootenai Formation, and 1.3 meters per year for the Lance-Fox Hills aquifer.

Montana, North Dakota, South Dakota, Wyoming↗

USGS2012

Biological assessment and streambed-sediment chemistry of streams in the Indianapolis metropolitan area, Indiana, 2003–2008

During 2003–2008, the U.S. Geological Survey sampled 13 sites in the Indianapolis metropolitan area in Indiana for benthic invertebrates, fish communities, and streambed-sediment chemistry. Data from seven White River sites and six tributary sites complement surface-water chemistry data collected by the Indianapolis Department of Public Works. The information is being used to assess changes in water quality in conjunction with the City's programs to reduce combined sewer overflows and other point and nonpoint sources of pollution in the Indianapolis area. During the study, 233 benthic-invertebrate taxa were identified from which the Ephemeroptera, Plecoptera, and Trichoptera (EPT) Index, the Hilsenhoff Biotic Index (HBI), and the Invertebrate Community Index (ICI) were calculated. EPT index scores ranged from 2 to 16 on the White River and from 2 to 17 on the tributaries. EPT index scores indicate that these pollution-intolerant taxa are more prevalent upstream from and away from the combined-sewer areas of Indianapolis. HBI scores from sites on the White River ranged from 4.67 (good) to 9.55 (very poor), whereas on the tributaries, scores ranged from 4.21 (very good) to 8.14 (poor). Lower HBI scores suggest that less organic pollution was present and, like the EPT scores, indicate better conditions where combined-sewer overflows (CSOs) are not present. Similarly, ICI scores indicated better conditions upstream from the CSO outfalls on the White River. White River scores ranged from 12 to 46, where higher ICI scores indicate better conditions in the benthic-invertebrate community. ICI scores at the tributary sites ranged from 12 to 52, with the highest scores on streams without CSOs.

Indiana↗

USGS2012

Streamflow gain and loss and water quality in the upper Nueces River Basin, south-central Texas, 2008-10

The U.S. Geological Survey-in cooperation with the U.S. Army Corps of Engineers, The Nature Conservancy, the Real Edwards Conservation and Reclamation District, and the Texas Parks and Wildlife Department-investigated streamflow gain and loss and water quality in the upper Nueces River Basin, south-central Texas, specifically in the watersheds of the West Nueces, Nueces, Dry Frio, Frio, and Sabinal Rivers upstream from the Edwards aquifer outcrop. Streamflow in these rivers is sustained by groundwater contributions (for example, from springs) and storm runoff from rainfall events. To date (2012), there are few data available that describe streamflow and water-quality conditions of the rivers within the upper Nueces River Basin. This report describes streamflow gain-loss characteristics from three reconnaissance-level synoptic measurement surveys (hereinafter referred to as "surveys") during 2008-10 in the upper Nueces River Basin. To help characterize the hydrology, groundwater-level measurements were made, and water-quality samples were collected from both surface-water and groundwater sites in the study area from two surveys during 2009-10. The hydrologic (streamflow, springflow, and groundwater) measurements were made during three reconnaissance-level synoptic measurement surveys occurring in July 21-23, 2008; August 8-18, 2009; and March 22-24, 2010. These survey periods were selected to represent different hydrologic conditions. Streamflow gains and losses were based on streamflow and springflow measurements made at 74 sites in the study area, although not all sites were measured during each survey. Possible water chemistry relations among sample types (streamflow, springflow, or groundwater), between surveys, and among watersheds were examined using water-quality samples collected from as many as 20 sites in the study area. During the three surveys, reaches of gaining, losing, or no verifiable change in streamflow were observed in the watersheds in the study area. Reaches of generally consistent gaining or losing streamflow were identified in the Nueces, Frio, and Sabinal River watersheds. The water-quality data indicate that the streamflow, springflow, and groundwater have similar major ion chemical characteristics and generally can be categorized as a calcium-carbonate water type. Those data also indicate that the major ion chemistry was similar during the 2009 and 2010 surveys. Graphical comparisons among ratios of major ions, trace elements, and isotopes (for example, magnesium/calcium ratios to strontium isotopic ratios) indicate that samples collected from each watershed generally clustered together. Determining the source areas and other possible contributors on the basis of these data is not possible because of the small sample size of the water-quality dataset (both in number of samples and spatial distribution of samples). The different relations among the water-quality data indicate that the surface water in the different watersheds is likely influenced by differences in source areas, geochemical evolution, groundwater flow paths and residence time, local stratigraphy, or some combination thereof.

Texas↗

USGS2002

Three-dimensional measurements of flow in uncased wells completed in basalt, Mountain Home Air Force Base, Idaho, March 2000

Several ground-water monitoring wells on the Mountain Home Air Force Base in southwestern Idaho were constructed in February 2000 to replace existing monitoring wells that became ineffective as a result of declining water levels. Upon completion of the replacement wells, borehole geophysical logs were collected, including natural gamma radiation, electromagnetic induction, caliper, fluid temperature, and resistivity. A prototype borehole acoustic doppler velocimeter (B-ADV) was used to make experimental three-dimensional measurements of lateral and vertical flow in two of the replacement wells, MW11–2 and MW3–2, each 450 feet deep, to better understand ground-water flow in the basalt underlying this area. Measurements indicated two independent flow zones in each well: unit B, from about 380 to about 415 feet below land surface, and unit C, from about 415 to about 430 feet below land surface. In each well, direction of flow in unit B was north-northwest toward Canyon Creek and, in unit C, south-southwest toward the Snake River. Measurements also indicated downward intraborehole flow in both wells. Unit B appeared to represent a local-scale flow regime; unit C appeared to represent a regional flow regime. This information suggests the existence of a complex three-dimensional hydrogeologic setting that cannot be discriminated easily on conventional waterlevel maps. Although data from only two wells are insufficient to construct a conceptual model of the ground-water flow regime, these experimental results demonstrate the capability of the B-ADV to obtain detailed flow measurements that, combined with data from other types of geophysical logs, discrete measurements of hydraulic head, and water chemistry, would aid in future studies and management of the ground-water resources, including contaminant transport and remediation.

Idaho↗

USGS1994

Hydrogeology and selected water-quality aspects of the Hueco Bolson Aquifer at the Hueco Bolson Recharge Project area, El Paso, Texas

Samples of ground water and tertiary-treated water were evaluated to determine the distribution of injected water and trihalomethane compounds in the Hueco bolson aquifer near El Paso, Texas. Chloride and nitrate concentrations and oxygen-18/oxygen-16 (δ 18 O) values were used with end-member mixing analysis to estimate the fractional contributions of injected water, irrigation-affected water, saline ground water, and freshwater to ground-water chemistry. Several laterally continuous sand and gravel layers are the principal water-yielding lithologies in the aquifer. The potentiometric surface sloped toward the south and southwest during January 1990. Average linear ground-water velocities were as large as 1.4 feet per day near the zone of largest hydraulic conductivity and were substantially smaller farther south and east. Ground-water samples from as far as 2,900 feet from an injection well contained injectedwater tracers and trihalomethane compounds. Ground-water samples with injected-water tracers and no trihalomethane compounds may indicate infiltration from septic systems or oxidation ponds. Apparent breakthrough velocities of injected water in the aquifer ranged from 0.13 to 1.3 feet per day. Irrigation-affected water and saline water also were identified in water from several wells. Ground-water transport of bromoform and dibromochloromethane is attenuated relative to injected water, chloroform, and dichlorobromomethane. Microbial transformation of bromoform and dibromochloromethane probably was responsible for their disappearance from ground water. Chloroform and dichlorobromomethane concentrations were affected principally by advective and dispersive transport of injected water.

Texas↗

USGS1998

Water quality assessment of the Sacramento River Basin, California: Environmental setting and study design

This report describes the environmental setting and investigative activities of the Sacramento River Basin study unit of the National Water-Quality Assessment Program. The Sacramento River Basin is one of 60 study units located throughout the United States that has been scheduled for study as part of the National Water-Quality Assessment Program. The Sacramento River Basin is the most important source of freshwater in California. Water quality studies in the Sacramento River Basin study unit focus on the Sacramento Valley because it is here that the principal uses of water and potential impacts on water quality occur. Investigative activities include a network of surface water sites, where water chemistry and aquatic biological sampling are done, and a variety of ground water studies. In addition, investigations of the cycling and distribution of volatile organic compounds in the urban environment and the distribution of total and methyl mercury in the Sacramento River and tributaries will be completed.

California↗

USGS1995

Estimates of ground-water recharge rates for two small basins in central Nevada

Estimates of ground-water recharge rates developed from hydrologic modeling studies are presented for 3-Springs and East Stewart basins. two small basins (analog sites) located in central Nevada. The analog-site studies were conducted to aid in the estimation of recharge to the paleohydrologic regime associated with ground water in the vicinity of Yucca Mountain under wetter climatic conditions. The two analog sites are located to the north and at higher elevations than Yucca Mountain, and the prevailing (current) climatic conditions at these sites is thought to be representative of the possible range of paleoclimatic conditions in the general area of Yucca Mountain during the Quaternary. Two independent modeling approaches were conducted at each of the analog sites using observed hydrologic data on precipitation, temperature, solar radiation stream discharge, and chloride-ion water chemistry for a 6-year study period (October 1986 through September 1992). Both models quantify the hydrologic water-balance equation and yield estimates of ground-water recharge, given appropriate input data. The first model uses a traditional approach to quantify watershed hydrology through a precipitation-runoff modeling system that accounts for the spatial variability of hydrologic inputs, processes, and responses (outputs) using a dailycomputational time step. The second model is based on the conservative nature of the dissolved chloride ion in selected hydrologic environments, and its use as a natural tracer allows the computation of acoupled, water and chloride-ion, mass-balance system of equations to estimate available water (sum ofsurface runoff and groundwater recharge). Results of the modeling approaches support the conclusion that reasonable estimates of average-annual recharge to ground water range from about 1 to 3 centimeters per year for 3-Springs basin (the drier site), and from about 30 to 32 centimeters per year for East Stewart basin (the wetter site). The most reliable results are those derived from a reduced form of the chloride-ion model because they reflect integrated, basinwide processes in terms of only three measured variables: precipitation amount, precipitation chemistry, and streamflow chemistry.

Nevada↗